Cited 43 time in
Synthesis and characterization of poly(benzodithiophene) derivative for organic thin film transistors
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dang, Thi Tuyet Mai | - |
| dc.contributor.author | Park, Sung-Jin | - |
| dc.contributor.author | Park, Jong-Won | - |
| dc.contributor.author | Chung, Dae-Sung | - |
| dc.contributor.author | Park, Chan Eon | - |
| dc.contributor.author | Kim, Yun-Hi | - |
| dc.contributor.author | Kwon, Soon-Ki | - |
| dc.date.accessioned | 2022-12-27T06:51:35Z | - |
| dc.date.available | 2022-12-27T06:51:35Z | - |
| dc.date.issued | 2007-11 | - |
| dc.identifier.issn | 0887-624X | - |
| dc.identifier.issn | 1099-0518 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/28245 | - |
| dc.description.abstract | Poly{2,6-bis(3-dodecylthiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene] (PTBT) was synthesized, via oxidative polymerization by oxidative agent (FeCl3). The mole ratio of FeCl3 and monomer (3.5: 1), and keeping low temperature during the dropping of diluted catalyst were very important for the polymerization without crosslinking. The PTBT was confirmed by H-1 NMR, FTIR spectra, and elemental analysis. The PTBT has very good solubility in organic solvents such as chloroform, tetrahydrofuran, etc, and good thermal stability with T-g of 164 degrees C. The PTBT shows UV-optical absorption at 406 nm and photoluminescence (PL) spectroscopy at 504 mn in a film. The highest occupied molecular orbital (HOMO) energy of the polymer is -5.71 eV by measuring cyclic voltammetry (CV). A solution-processed polymer thin film transistor device shows a mobility of 3 X 10(-5) - 8 X 10(-5) cm(2) V-1 s(-1), and an on/off current ratio of 10(4). (c) 2007 Wiley Periodicals, Inc. | - |
| dc.format.extent | 8 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | John Wiley & Sons Inc. | - |
| dc.title | Synthesis and characterization of poly(benzodithiophene) derivative for organic thin film transistors | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1002/pola.22272 | - |
| dc.identifier.scopusid | 2-s2.0-35748965603 | - |
| dc.identifier.wosid | 000250788600024 | - |
| dc.identifier.bibliographicCitation | Journal of Polymer Science, Part A: Polymer Chemistry, v.45, no.22, pp 5277 - 5284 | - |
| dc.citation.title | Journal of Polymer Science, Part A: Polymer Chemistry | - |
| dc.citation.volume | 45 | - |
| dc.citation.number | 22 | - |
| dc.citation.startPage | 5277 | - |
| dc.citation.endPage | 5284 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Polymer Science | - |
| dc.relation.journalWebOfScienceCategory | Polymer Science | - |
| dc.subject.keywordPlus | BLUE | - |
| dc.subject.keywordPlus | POLYMERS | - |
| dc.subject.keywordAuthor | benzodithiophene | - |
| dc.subject.keywordAuthor | conducting polymers | - |
| dc.subject.keywordAuthor | OTFT | - |
| dc.subject.keywordAuthor | oxidative polymerization | - |
| dc.subject.keywordAuthor | solution properties | - |
| dc.subject.keywordAuthor | spin coating | - |
| dc.subject.keywordAuthor | thiophene | - |
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